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Schmid Metaphyseal Chondrodysplasia
Schmid metaphyseal chondrodysplasia
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Diseases and disorders
(15)
Raine syndrome
Chondrodysplasia punctata, rhizomelic
Osteochondropathy
Osteochond- rodysplasia
Short rib-polydactyly syndrome
Short rib-polydactyly syndrome
Metaphyseal dysplasia
Bethlem myopathy
Pelger-Huet anomaly
Osteopoikilosis
Muscular dystrophy
Epidermolysis bullosa dystrophica
Multiple sulfatase deficiency
Cartilage hair hypoplasia
Dysostosis
Macrocephaly
more...
Congenital disorders
(10)
Achondrogenesis type 2
Fibrochondrogenesis
Achondrogenesis type 1B
Buschke-Ollendorff syndrome
Achondrogenesis
Achondrogenesis
Ehlers Danlos Syndrome
Marinesco sjogren syndrome
Congenital malformations
Bethlem myopathy
Macrocephaly
more...
Rare diseases
(12)
Atelosteogenesis, type II
Boomerang dysplasia
Barraquer-Simons Syndrome
Marshall syndrome
Multiple epiphyseal dysplasia
Multiple epiphyseal dysplasia
Lelis syndrome
Epidermolytic hyperkeratosis
Thanatophoric dysplasia
Stickler syndrome
Fibrochondrogenesis
Raine syndrome
Multiple sulfatase deficiency
more...
Autosomal recessive disorders
(8)
Otospondyl- omegaepiphyseal dysplasia
Chondrodystrophy
Diastrophic dysplasia
Atelosteogenesis, type II
Fibrochondrogenesis
Fibrochondrogenesis
Raine syndrome
Multiple sulfatase deficiency
Cartilage hair hypoplasia
more...
Syndromes
(13)
Laminopathy
Alport syndrome
Maffucci syndrome
Pfeiffer syndrome
Androgen insensitivity syndrome
Androgen insensitivity syndrome
Myelodysplastic syndromes
Raine syndrome
Buschke-Ollendorff syndrome
Barraquer-Simons Syndrome
Marshall syndrome
Ehlers Danlos Syndrome
Lelis syndrome
Stickler syndrome
more...
Genodermatoses
Chondrodysplasia punctata, rhizomelic
Epidermolysis bullosa dystrophica
Multiple sulfatase deficiency
Lelis syndrome
Cartilage hair hypoplasia
Epidermolytic hyperkeratosis
Pfeiffer syndrome
Muscular disorders
(23)
Myopathy
Myotubular myopathy
Arthrogryposis
Central core disease
Chronic progressive external ophthalmoplegia
Chronic progressive external ophthalmoplegia
Congenital myopathy
Diastasis recti
Inclusion body myositis
Laminopathy
Macrophagic myofasciitis
Metabolic myopathy
Mitochondrial myopathy
Muscular dystrophy
Myokmia
Nemaline myopathy
Orofacial myological disorders
Pelvic Floor Muscle Disorder
Polymyositis
Thyrotoxic myopathy
Torticollis
Writer's cramp
X-linked myotubular myopathy
Zenker's degeneration
more...
Skeletal system
Skeletal disorders
Osseous
Metaphyseal
Hypochondroplasia
Skeletal disorders
Ollier disease
Hereditary multiple exostoses
Chondrodystrophy
Growth disorders
Metatropic dwarfism
Achondroplasia
Hypochondroplasia
Symptoms
Short stature
Short arms and legs
Bowed legs
Mental retardation
Genetic disorders
(34)
Hypochondrogenesis
Spondylometaphyseal dysplasia
Fukuyama type muscular dystrophy
Spondyloepiphyseal dysplasia congenita
Collagenopathy, types II and XI
Collagenopathy, types II and XI
McCune Albright syndrome
Atelosteogenesis, type II
Fibrochondrogenesis
Raine syndrome
Boomerang dysplasia
Buschke-Ollendorff syndrome
Laminopathy
Barraquer-Simons Syndrome
Otospondyl- omegaepiphyseal dysplasia
Bethlem myopathy
Pelger-Huet anomaly
Marshall syndrome
Muscular dystrophy
Ehlers Danlos Syndrome
Multiple epiphyseal dysplasia
Achondroplasia
Alport syndrome
Multiple sulfatase deficiency
Lelis syndrome
Hereditary multiple exostoses
Cartilage hair hypoplasia
Hypochondroplasia
Thanatophoric dysplasia
Chondrodystrophy
Diastrophic dysplasia
Stickler syndrome
Pfeiffer syndrome
Androgen insensitivity syndrome
Inherited diseases
more...
Medical condition
(49)
Metaphyseal chondrodysplasia schmid type
Chondromatous
Antley-bixler syndrome
Ichthyosis bullosa of siemens
Camurati engelmann disease
Camurati engelmann disease
Jansen type metaphyseal chondrodysplasia
Morvan disease
Enchondromatosis
Steatocystoma multiplex
Bullous pemphigoid
Meniscus tear
Achondrogenesis type 2
Fibrochondrogenesis
Raine syndrome
Boomerang dysplasia
Chondrodysplasia punctata, rhizomelic
Hypochondrogenesis
Osteochond- rodysplasia
Short rib-polydactyly syndrome
Bethlem myopathy
Ollier disease
Pelger-Huet anomaly
Spondylometaphyseal dysplasia
Osteopoikilosis
Marshall syndrome
Fukuyama type muscular dystrophy
Muscular dystrophy
Spondyloepiphyseal dysplasia congenita
Metatropic dwarfism
Ehlers Danlos Syndrome
Epidermolysis bullosa dystrophica
Multiple epiphyseal dysplasia
Achondroplasia
Alport syndrome
Maffucci syndrome
Marinesco sjogren syndrome
Hereditary multiple exostoses
Hypochondroplasia
Thanatophoric dysplasia
Chondrodystrophy
Myopathy
Myotubular myopathy
Diastrophic dysplasia
Dysostosis
Stickler syndrome
Bowed legs
Androgen insensitivity syndrome
Myelodysplastic syndromes
Mental retardation
more...
See also
(20)
Keratinopathy
Scleroprotein
Collagen, type X, alpha 1
Mullerian duct
SLC26A2
SLC26A2
COL2A1 gene
Autosomal dominant
Autosomal recessive
Dysplasia
Autoimmune
COL11A1
Type II collagen
Hellmut Schmid
Mycosis fungoides
PMID
Genetic counseling
Inherited diseases
Integument
Mutations
Subcutaneous tissue
more...
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